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89 Possible Causes for Huntington's Disease, Progressive Action Tremor

  • Parkinson's Disease

    […] reduction in speed and amplitude of repetitive actions) and at least one of the following: (i) muscular rigidity, (ii) 4–6 Hz rest tremor and (iii) postural instability not[doi.org] Assessment of Caregiver Burden in Huntington's Disease. Yu M, Tan K, Koloms K, Bega D. J Huntingtons Dis. 2019;8(1):111-114. doi: 10.3233/JHD-180326.[parkinsons.northwestern.edu] Click on the following links to learn more about the conditions we treat: Essential Tremor Huntington's Disease MSA Dystonia PSP Watch this video to learn about focused ultrasound[umm.edu]

  • Dentatorubral-Pallidoluysian Atrophy

    Seite 190 - Bradykinesia (slowness of initiation of voluntary movement with progressive reduction in speed and amplitude of repetitive actions) • And at least one of the following[books.google.de] We focus on Huntington's disease (HD) and Dentatorubral-pallidoluysian atrophy (DRPLA) as models for this family of diseases, since they have striking similarities and also[ncbi.nlm.nih.gov] Nature 352, 77–79 (1991). 15 The Huntington's Disease Collaborative Research Group.[doi.org]

  • Movement Disorder

    Tremor: Descriptions of tremors progressed from Galen's definition in the 2nd century; to Galileo's physiologic tremor in 1610; separation of involuntary movements during[ncbi.nlm.nih.gov] Huntington’s Disease We are a Huntington’s Disease Society of America Center of Excellence for the Rocky Mountain region.[movementdisorderscenter.org] ’s disease Parkinson’s disease Torticollis Tourette’s syndrome IU Health experts have advanced expertise in Parkinson's disease and Huntington's disease.[iuhealth.org]

  • Neurodegenerative Disorder

    tremor, myoclonus, hyper-reflexia, and focal limb dystonia.[aao.org] The disease is associated with a CAG trinucleotide-repeat expansion in the Huntington gene (IT15) on chromosome 4p16.3.[ncbi.nlm.nih.gov] Abstract Huntington's disease (HD) is an autosomal dominantly inherited, and currently untreatable, neuropsychiatric disorder.[ncbi.nlm.nih.gov]

  • Benign Familial Chorea

    It is an action tremor occurring during activity and is of greater amplitude when reaching for a target.[academic.sun.ac.za] HD, Huntington’s disease family history Huntington’s disease incidence late onset new mutation rate Statistics from Altmetric.com Request Permissions If you wish to reuse[jnnp.bmj.com] Read more about the symptoms of Huntington's disease.[nhs.uk]

  • Senile Chorea

    It is an action tremor occurring during activity and is of greater amplitude when reaching for a target.[academic.sun.ac.za] There is a widely held belief that most patients presenting with senile chorea have late-onset Huntington's disease (HD) with an unknown family history.[ncbi.nlm.nih.gov] Abstract A simple and reproducible method of polymerase chain reaction (PCR) assay was established to detect trinucleotide repeat expansion for Huntington's disease (HD) using[ncbi.nlm.nih.gov]

  • Hemiballismus

    It is an action tremor occurring during activity and is of greater amplitude when reaching for a target.[academic.sun.ac.za] Joohi Jimenez-Shahed and Joseph Jankovic, Tetrabenazine for treatment of chorea associated with Huntington's disease and other potential indications, Expert Opinion on Orphan[oadoi.org] It is a slowly progressive and permanent disorder. The amplitude increases in hyperadrenergic situations.[academic.sun.ac.za]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Spinocerebellar ataxia type 12 (SCA12) is an autosomal dominant disorder characterized by action tremor of the upper extremities progressing to ataxia and other cerebellar[chginc.org] The Huntington’s disease-like syndromes: what to consider in patients with a negative Huntington’s disease gene test.[ncbi.nlm.nih.gov] Disease-Like Syndromes Huntington's disease-like disorders are a rare cause of chorea (Table 1 ).[movementdisorders.org]

  • Adult-Onset Cervical Dystonia Type DYT23

    […] to other body sites and time course of progression Occurrence of dystonia at rest, with any specific voluntary action, or posture maintenance Presence or absence of tremor[misc.medscape.com] "Dystonia in Huntington's disease: Prevalence and clinical characteristics". Movement Disorders. 14 (1): 95–101. doi : 10.1002/1531-8257(199901)14:1 3.0.CO;2-8.[wikivisually.com] The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.[ncbi.nlm.nih.gov]

  • Neuronal Intranuclear Inclusion Disease

    He was found to have significant action and sustention tremor, bilateral lower leg weakness (tibialis anterior), decreased deep tendon reflexes and pes planus.[path.upmc.edu] Diagnostic considerations for juvenile onset Parkinsonism (onset at 21 years of age) include juvenile Huntington disease, Wilson disease, dentatorubral-pallidoluysian atrophy[ncbi.nlm.nih.gov] "We work in a very competitive and cooperative environment in Huntington's disease," Aronin remarks.[the-scientist.com]

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